The Influence of Sulfate‐Doping on the Nature of V Sites in VOx/TiO2 Catalysts

EPR, UV/Vis and FTIR spectroscopy as well as thermal analysis (TA/MS) were applied to study the influence of sulfate species present in the anatase support on the specific nature of VO_x species in supported VO_x/TiO₂ catalysts. Those sulfate species modify the local structure of the supported vanadyl species and lead to the formation of two types of VO²⁺ sites instead of only one type being formed on sulfate‐free anatase. EPR and FTIR spectroscopic measurements revealed that a part of the VO²⁺ species are directly bound to the surface sulfate species. By TA/MS it was found that SO₂ is released at lower temperature from VO_x/TiO₂ in comparison to the vanadium‐free support. The direct bonding between sulfate and VO_x species stabilizes the latter on the surface of VO_x/TiO₂ resulting in three effects: 1) a higher V site dispersion in comparison to sulfate‐free TiO₂, 2) a better resistance of surface vanadyls against diffusion into the bulk of the support and 3) a much faster reoxidation of reduced V sites than observed on sulfate‐free TiO₂.     

Mechanical properties of single motor molecules studied by three-dimensional thermal force probing in optical tweezers.

A new method combining three-dimensional (3D) force measurements in an optical trap with the analysis of thermally induced (Brownian) position fluctuations of a trapped probe was used to investigate the mechanical properties of a single molecule, the molecular motor kinesin. One kinesin molecule attached to the probe was bound in a rigorlike state to one microtubule. The optical trap was kept weak to measure the thermal forces acting on the probe, which were mainly counterbalanced by the kinesin tether. The stiffness of kinesin during stretching and compression with respect to its backbone axis were measured. Our results indicate that a section of kinesin close to the motor domain is the dominating element in the flexibility of the motor structure. The experiments demonstrate the power of 3D thermal fluctuation analysis to characterize mechanical properties of individual motor proteins and indicate its usefulness to study single molecule in general     

Mesogene-polymer backbone coupling in side-chain polymer liquid crystals,studied by high magnetic-field-induced alignment

We show that cooling side chain polymer liquid crystals in a magnetic field, from the isotropic to nematic and subsequently to the glass phase, results in a macroscopically ordered, transparent, and strongly birefringent material. The aligned samples retain their properties after the field is removed and can be dealigned only by heating them to the isotropic phase. To induce alignment, a threshold field B(th) is necessary, which strongly depends on the chemical structure details. B(th) reflects the strength of mesogene-polymer backbone coupling, and we will show that this interaction is responsible for the stability of the induced alignment at zero field.     

Multiple imaging axis microscopy improves resolution for thick-sample applications

The multiple imaging axis microscope (MIAM) is a wide-field optical microscope that observes a sample simultaneously from multiple directions without requiring the sample to be rotated or tilted. The prototype is capable of high-resolution imaging of the interior of a 300-microm-diameter sample consisting of fluorescent microbeads suspended in an agarose gel. Compared with a single-axis system, the MIAM can achieve a reduction of the axial point-spread function elongation by a factor of 5.8 and a 3.5-fold improvement in volume resolution by simple linear image combination techniques.     

Synthesis of a eta 2-2,3-diphosphabutadiene complex of zerovalent platinum from the corresponding eta 2-phosphaalkyne complex

Hydrozirconation of the eta 2-phosphaalkyne complex [Pt(dppe)(eta 2-tBuCP)] with [ZrHCl(eta 5-C5H5)2], followed by treatment with the chlorophosphaalkene ClP=C(SiMe3)2 affords the eta 2-2,3-diphosphabutadiene complex [Pt(dppe)(eta 2-tBuC(H)=PP=C(SiMe3)2]. In the presence of [Pt(PPh3)2] the latter undergoes an addition reaction with water to afford the structurally characterised Pt(II) complex [Pt(dppe)(tBuCH2P(O)HPC(SiMe3)2].     

Nucleon transfer reactions to rotational states induced by206, 208Pb projectiles

In a systematic study of nucleon transfer reactions accompanied by Coulomb excitation we have bombarded¹⁵²Sm,¹⁶⁰Gd and²³²Th with^{206, 208}pb beams at incident energies close to the Coulomb barrier. Particle-gamma coincidence techniques were used to identify excited states of reaction products populated through inelastic scattering and in nucleon transfer reactions. One-neutron stripping and pick-up reactions on¹⁵²Sm were observed leading to known states of the rotation alignedi _13/2-bands in¹⁵³Sm and¹⁵¹Sm. In the¹⁶⁰Gd+^{206, 208}Pb systems no significant population of low lying states of product nuclei was found in the nucleon-transfer channels. Large cross sections were observed for one- and two-neutron pick-up from²³²Th at an incident energy of 6.4 MeV/u. Around the grazing angle they are of the same order of magnitude as the cross section measured for inelastic scattering. The results are analyzed in the framework of semiclassical models.     

Triaxiality andγ-softness in196Pt

The nuclear level structure and electromagnetic properties of¹⁹⁶Pt were investigated withγ-spectroscopic techniques using multiple Coulomb excitation by²⁰⁸Pb projectiles. Particle-γ, and particle-γ-γ coincidences were measured over a wide range of scattering angles.E2-transition moments and static quadrupole moments have been determined by a comparison of experimental scattering-angle dependentγ yields with calculated yields in a largely model-independent procedure. The results are compared with different theoretical models: the Asymmetric-Rotor Model, the Generalized Collective Model, and the Interacting Boson Model. The best agreement is obtained with the Generalized Collective Model representing a triaxial nucleus which is soft in theγ degree of freedom.